http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1230208-B1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C209-02
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07B61-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C211-52
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C209-00
filingDate 2000-03-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2006-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6a39acff029111df2cca544cda4be43b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_06eab14bfb7003153120d9138fea2d39
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5f7c422cb2c25e8a71e24dfd9c6806d1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_42ae75293c4bcdea9cf065f770297fc4
publicationDate 2006-06-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1230208-B1
titleOfInvention Manufacturing method for 4-nitrosoaniline from urea and nitrobenzene
abstract Disclosed herein is a method for preparing 4-nitrosoaniline, comprising reacting urea and nitrobenzene in a polar organic solvent in the presence of a base at a temperature of room temperature to 150 °C. The method uses a relatively cheap urea and nitrobenzene as the raw materials, and also a relatively cheap base, thereby decreasing the manufacturing cost. Urea used as an amine donor is excellent in a reactivity to nitrobenzene, and a reaction intermediate is unstable as compared with 4-(4-nitrophenyl)benzamide to easily decompose into 4-nitroaniline and 4-nitrosoaniline. This allows a reaction time and a process time to be shortened. Moreover, the method is advantageous in that waste hazardous to the environment is not produced as a byproduct.
priorityDate 1999-11-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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